Detalhe da pesquisa
1.
Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 622(7984): 784-793, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37821707
2.
Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience.
Am J Hum Genet
; 109(9): 1582-1590, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36055210
3.
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 626(8001): E18, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38332034
4.
First mitochondrial genome-wide association study with metabolomics.
Hum Mol Genet
; 31(19): 3367-3376, 2022 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34718574
5.
A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank.
Am J Hum Genet
; 108(4): 669-681, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33730541
6.
De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
Proc Natl Acad Sci U S A
; 117(5): 2560-2569, 2020 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31964835
7.
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Mol Psychiatry
; 26(9): 5239-5250, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33483695
8.
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Proc Natl Acad Sci U S A
; 115(2): 379-384, 2018 01 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29279374
9.
Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.
Genome Res
; 26(4): 417-26, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26916109
10.
Helmsman: fast and efficient mutation signature analysis for massive sequencing datasets.
BMC Genomics
; 19(1): 845, 2018 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30486787
11.
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Mol Psychiatry
; 26(9): 5251, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33674754
12.
Robust and Powerful Affected Sibpair Test for Rare Variant Association.
Genet Epidemiol
; 39(5): 325-33, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25966809
13.
Long runs of homozygosity are enriched for deleterious variation.
Am J Hum Genet
; 93(1): 90-102, 2013 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23746547
14.
The influence of genomic context on mutation patterns in the human genome inferred from rare variants.
Genome Res
; 23(12): 1974-84, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23990608
15.
Comparing variant calling algorithms for target-exon sequencing in a large sample.
BMC Bioinformatics
; 16: 75, 2015 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25884587
16.
A quantitative comparison of the similarity between genes and geography in worldwide human populations.
PLoS Genet
; 8(8): e1002886, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22927824
17.
Metabolic syndrome in bipolar disorder and schizophrenia: dietary and lifestyle factors compared to the general population.
Bipolar Disord
; 16(3): 277-88, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24330321
18.
Psychiatric genetics: progress amid controversy.
Nat Rev Genet
; 9(7): 527-40, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18560438
19.
Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.
PLoS Genet
; 7(6): e1002134, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21738484
20.
A Stacking Framework for Polygenic Risk Prediction in Admixed Individuals.
medRxiv
; 2024 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38434717